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Influenza Virus-like Particle Containing Two Different Subtypes of Hemagglutinin Confers Protection in Mice Against Lethal Challenge With A/PR8 (H1N1) and A/HK (H3N2) Viruses
BACKGROUND: Preventing the seasonal or pandemic outbreak of influenza can be powerful and cost-effective. OBJECTIVES: In this study, we constructed a novel virus-like particle (VLP) platform that contains two hemagglutinin (HA) subtypes and evaluated immunogenicity of constructed VLP in mice. MATERI...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Kowsar
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589784/ https://www.ncbi.nlm.nih.gov/pubmed/23487492 http://dx.doi.org/10.5812/ircmj.6252 |
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author | Rezaei, Farhad Mirshafiey, Abbas Shahmahmoodi, Shohreh Shoja, Zabihollah Ghavami, Nastaran Mokhtari-Azad, Talat |
author_facet | Rezaei, Farhad Mirshafiey, Abbas Shahmahmoodi, Shohreh Shoja, Zabihollah Ghavami, Nastaran Mokhtari-Azad, Talat |
author_sort | Rezaei, Farhad |
collection | PubMed |
description | BACKGROUND: Preventing the seasonal or pandemic outbreak of influenza can be powerful and cost-effective. OBJECTIVES: In this study, we constructed a novel virus-like particle (VLP) platform that contains two hemagglutinin (HA) subtypes and evaluated immunogenicity of constructed VLP in mice. MATERIALS AND METHODS: This recombinant candidate vaccine model resulted in the expression of two HAs of H1N1 and H3N2 subtypes co-localized within a VLP. Following infection of insect cells with recombinant baculovirus co-expressing H1, H3 and M1 proteins, VLPs with size of 80–120 nm were self-assembled, budding, and released into the insect culture medium. The resulting VLPs which contained two different subtypes of hemagglutinin were purified by ultracentrifugation. The immunogenicity of VLPs was evaluated in mice following immunization. RESULTS: Our data showed that vaccination using VLPs elicited robust levels of serum IgG, and viral neutralizing antibodies against A/PR8 (H1N1) and A/HK (H3N2) viruses. Following challenge with lethal dose of A/PR8 (H1N1) and A/HK (H3N2, vaccinated mice were protected, displaying no sign of weight loss and mortality compared to non-vaccinated control mice. CONCLUSIONS: VLPs can serve as a promising vaccination strategy to control influenza virus. |
format | Online Article Text |
id | pubmed-3589784 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Kowsar |
record_format | MEDLINE/PubMed |
spelling | pubmed-35897842013-03-13 Influenza Virus-like Particle Containing Two Different Subtypes of Hemagglutinin Confers Protection in Mice Against Lethal Challenge With A/PR8 (H1N1) and A/HK (H3N2) Viruses Rezaei, Farhad Mirshafiey, Abbas Shahmahmoodi, Shohreh Shoja, Zabihollah Ghavami, Nastaran Mokhtari-Azad, Talat Iran Red Crescent Med J Research Article BACKGROUND: Preventing the seasonal or pandemic outbreak of influenza can be powerful and cost-effective. OBJECTIVES: In this study, we constructed a novel virus-like particle (VLP) platform that contains two hemagglutinin (HA) subtypes and evaluated immunogenicity of constructed VLP in mice. MATERIALS AND METHODS: This recombinant candidate vaccine model resulted in the expression of two HAs of H1N1 and H3N2 subtypes co-localized within a VLP. Following infection of insect cells with recombinant baculovirus co-expressing H1, H3 and M1 proteins, VLPs with size of 80–120 nm were self-assembled, budding, and released into the insect culture medium. The resulting VLPs which contained two different subtypes of hemagglutinin were purified by ultracentrifugation. The immunogenicity of VLPs was evaluated in mice following immunization. RESULTS: Our data showed that vaccination using VLPs elicited robust levels of serum IgG, and viral neutralizing antibodies against A/PR8 (H1N1) and A/HK (H3N2) viruses. Following challenge with lethal dose of A/PR8 (H1N1) and A/HK (H3N2, vaccinated mice were protected, displaying no sign of weight loss and mortality compared to non-vaccinated control mice. CONCLUSIONS: VLPs can serve as a promising vaccination strategy to control influenza virus. Kowsar 2013-01-05 2013-01 /pmc/articles/PMC3589784/ /pubmed/23487492 http://dx.doi.org/10.5812/ircmj.6252 Text en Copyright © 2013, Iranian Red Crescent Medical Journal http://creativecommons.org/licenses/by/3/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Rezaei, Farhad Mirshafiey, Abbas Shahmahmoodi, Shohreh Shoja, Zabihollah Ghavami, Nastaran Mokhtari-Azad, Talat Influenza Virus-like Particle Containing Two Different Subtypes of Hemagglutinin Confers Protection in Mice Against Lethal Challenge With A/PR8 (H1N1) and A/HK (H3N2) Viruses |
title | Influenza Virus-like Particle Containing Two Different Subtypes of Hemagglutinin Confers Protection in Mice Against Lethal Challenge With A/PR8 (H1N1) and A/HK (H3N2) Viruses |
title_full | Influenza Virus-like Particle Containing Two Different Subtypes of Hemagglutinin Confers Protection in Mice Against Lethal Challenge With A/PR8 (H1N1) and A/HK (H3N2) Viruses |
title_fullStr | Influenza Virus-like Particle Containing Two Different Subtypes of Hemagglutinin Confers Protection in Mice Against Lethal Challenge With A/PR8 (H1N1) and A/HK (H3N2) Viruses |
title_full_unstemmed | Influenza Virus-like Particle Containing Two Different Subtypes of Hemagglutinin Confers Protection in Mice Against Lethal Challenge With A/PR8 (H1N1) and A/HK (H3N2) Viruses |
title_short | Influenza Virus-like Particle Containing Two Different Subtypes of Hemagglutinin Confers Protection in Mice Against Lethal Challenge With A/PR8 (H1N1) and A/HK (H3N2) Viruses |
title_sort | influenza virus-like particle containing two different subtypes of hemagglutinin confers protection in mice against lethal challenge with a/pr8 (h1n1) and a/hk (h3n2) viruses |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589784/ https://www.ncbi.nlm.nih.gov/pubmed/23487492 http://dx.doi.org/10.5812/ircmj.6252 |
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